Hossein Darvish

3.6k total citations
96 papers, 1.3k citations indexed

About

Hossein Darvish is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Hossein Darvish has authored 96 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 44 papers in Genetics and 15 papers in Cell Biology. Recurrent topics in Hossein Darvish's work include Genetics and Neurodevelopmental Disorders (22 papers), Autism Spectrum Disorder Research (12 papers) and Genomics and Rare Diseases (10 papers). Hossein Darvish is often cited by papers focused on Genetics and Neurodevelopmental Disorders (22 papers), Autism Spectrum Disorder Research (12 papers) and Genomics and Rare Diseases (10 papers). Hossein Darvish collaborates with scholars based in Iran, United States and Germany. Hossein Darvish's co-authors include Coro Paisán‐Ruiz, Mina Ohadi, Abbas Tafakhori, Gholam Ali Shahidi, Babak Emamalizadeh, Javad Jamshidi, Siamak Karkheiran, Ruth H. Walker, Vladimir Makarov and Catharine E. Krebs and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Scientific Reports.

In The Last Decade

Hossein Darvish

93 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Hossein Darvish Iran 18 609 332 270 259 208 96 1.3k
Zhengmao Hu China 25 1000 1.6× 535 1.6× 430 1.6× 226 0.9× 207 1.0× 127 1.9k
Pascale Saugier-Véber France 28 1.1k 1.9× 672 2.0× 437 1.6× 257 1.0× 156 0.8× 82 2.3k
Alexandra Benchoua France 19 1.1k 1.8× 169 0.5× 470 1.7× 165 0.6× 105 0.5× 34 1.6k
Hiroyuki Koizumi Japan 19 687 1.1× 192 0.6× 382 1.4× 79 0.3× 323 1.6× 54 1.5k
Guy M. Lenk United States 23 616 1.0× 191 0.6× 339 1.3× 220 0.8× 620 3.0× 38 1.7k
Roberta Biancheri Italy 31 1.3k 2.1× 377 1.1× 350 1.3× 196 0.8× 339 1.6× 100 2.5k
Tarja Joensuu Finland 19 670 1.1× 344 1.0× 158 0.6× 141 0.5× 261 1.3× 31 1.3k
Tanjew Dittgen Germany 10 468 0.8× 137 0.4× 387 1.4× 148 0.6× 113 0.5× 10 1.0k
Francisco Martı́nez Spain 24 1.1k 1.8× 837 2.5× 301 1.1× 219 0.8× 130 0.6× 118 1.8k
Pedro Mancías United States 15 750 1.2× 149 0.4× 809 3.0× 380 1.5× 228 1.1× 37 1.7k

Countries citing papers authored by Hossein Darvish

Since Specialization
Citations

This map shows the geographic impact of Hossein Darvish's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hossein Darvish with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hossein Darvish more than expected).

Fields of papers citing papers by Hossein Darvish

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hossein Darvish. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hossein Darvish. The network helps show where Hossein Darvish may publish in the future.

Co-authorship network of co-authors of Hossein Darvish

This figure shows the co-authorship network connecting the top 25 collaborators of Hossein Darvish. A scholar is included among the top collaborators of Hossein Darvish based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hossein Darvish. Hossein Darvish is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Darvish, Hossein, et al.. (2023). A biallelic loss-of-function variant in TMEM147 causes profound intellectual disability and spasticity. Neurogenetics. 24(4). 311–316.
2.
Bahmanpour, Zahra, Somayeh Kazeminasab, Elham Alehabib, et al.. (2022). A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 24(1-2). 148–151. 2 indexed citations
3.
Emamalizadeh, Babak, et al.. (2021). Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations. International Ophthalmology. 41(10). 3269–3276. 3 indexed citations
4.
Alehabib, Elham, et al.. (2021). Clinical and molecular spectrum of P/Q type calcium channel Cav2.1 in epileptic patients. Orphanet Journal of Rare Diseases. 16(1). 461–461. 8 indexed citations
5.
Darvish, Hossein, Luís Azcona, Saghar Ghasemi Firouzabadi, et al.. (2021). ANXA1 with Anti‐Inflammatory Properties Might Contribute to Parkinsonism. Annals of Neurology. 90(2). 319–323. 8 indexed citations
6.
Fazeli, Walid, Somayeh Bakhtiari, Abbas Tafakhori, et al.. (2021). The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature. European Journal of Paediatric Neurology. 36. 7–13. 5 indexed citations
7.
Alehabib, Elham, et al.. (2020). Incomplete penetrance of MITF gene c.943C>T mutation in an extended family with Waardenburg syndrome type II. International Journal of Pediatric Otorhinolaryngology. 135. 110014–110014. 6 indexed citations
8.
Emamalizadeh, Babak, et al.. (2020). Analysis of polymorphism and function of GA repeat in RIT2 gene promoterAnalysis of polymorphism and function of GA repeat in RIT2 gene promoter in Parkinson’s disease. Research in Medicine. 44(4). 526–531. 1 indexed citations
9.
Bahmanpour, Zahra, et al.. (2020). A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome. International Ophthalmology. 41(2). 389–397. 5 indexed citations
10.
Darvish, Hossein, et al.. (2019). Features, genetics and their correlation in Jalili syndrome: a systematic review. Journal of Medical Genetics. 56(6). 358–369. 11 indexed citations
11.
Ghaedi, Hamid, et al.. (2019). Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome. Genes & Diseases. 7(4). 614–619. 2 indexed citations
12.
Darvish, Hossein, et al.. (2018). Molecular characterization of PRKN structural variations identified through whole‐genome sequencing. Molecular Genetics & Genomic Medicine. 6(6). 1243–1248. 6 indexed citations
13.
Darvish, Hossein, et al.. (2018). RIT2: responsible and susceptible gene for neurological and psychiatric disorders. Molecular Genetics and Genomics. 293(4). 785–792. 9 indexed citations
14.
Alehabib, Elham, Ehsan Esmaili Shandiz, Javad Jamshidi, et al.. (2017). Support for “Disease-Only” Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia. Genetic Testing and Molecular Biomarkers. 21(8). 485–490. 14 indexed citations
15.
Lima, Behnam Safarpour, Hamid Ghaedi, Narsis Daftarian, et al.. (2016). c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. European Journal of Medical Genetics. 59(2). 65–69. 6 indexed citations
16.
Khaniani, Mahmoud Shekari, Ehsan Esmaili Shandiz, Hormoz Ayromlou, et al.. (2016). Genetic Analysis of the ZNF512B , SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population. Genetic Testing and Molecular Biomarkers. 20(10). 629–632. 13 indexed citations
17.
Jamshidi, Javad, et al.. (2016). SNAP-25gene variations and attention-deficit hyperactivity disorder in Iranian population. Neurological Research. 38(11). 959–964. 1 indexed citations
18.
Jamshidi, Javad, Farkhondeh Pouresmaeili, Hossein Darvish, et al.. (2014). FABP9 Mutations Are Not Detected in Cases of Infertility due to Sperm Morphological Defects in Iranian Men. SHILAP Revista de lepidopterología. 2 indexed citations
19.
Movafagh, Abolfazl, Kiandokht Ghanati, Davar Amani, et al.. (2013). The structure Biology and Application of Phytohemagglutinin (PHA) in Phytomedicine: With special up-to-date references to lectins. Journal of paramedical sciences.. 4. 126–141. 9 indexed citations
20.
Movafagh, Abolfazl, et al.. (2013). Identification of homogeneously staining regions in leukemia patients. SHILAP Revista de lepidopterología. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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